Aubry L, Klein G, Martiel J L, Satre M
Laboratoire de Biologie Cellulaire (URA 1130 CNRS), Département de Biologie Moléculaire et Structurale, Grenoble, France.
J Cell Sci. 1993 Jul;105 ( Pt 3):861-6. doi: 10.1242/jcs.105.3.861.
The evolution of endo-lysosomal pH in Dictyostelium discoideum amoebae was examined during fluid-phase endocytosis. Pulse-chase experiments were conducted in nutritive medium or in non-nutritive medium using fluorescein labelled dextran (FITC-dextran) as fluid-phase marker and pH probe. In both conditions, efflux kinetics were characterized by an extended lag phase lasting for 45-60 min and corresponding to intracellular transit of FITC-dextran cohort. During the chase period, endosomal pH decreased during approximately 20 min from extracellular pH down to pH 4.6-5.0, then, it increased within the next 20-40 min to reach pH 6.0-6.2. It was only at this stage that FITC-dextran was released back into the medium with pseudo first-order kinetics. A vacuolar H(+)-ATPase is involved in endosomal acidification as the acidification process was markedly reduced in mutant strain HGR8, partially defective in vacuolar H(+)-ATPase and in parent type strain AX2 by bafilomycin A1, a selective inhibitor of this enzyme. Our data suggest that endocytic cargo is channeled from endosomes to secondary lysosomes that are actively linked to the plasma membrane via recycling vesicles.
在液相内吞作用过程中,研究了盘基网柄菌变形虫内溶酶体pH值的变化。使用荧光素标记的葡聚糖(FITC-葡聚糖)作为液相标记物和pH探针,在营养培养基或非营养培养基中进行脉冲追踪实验。在这两种情况下,流出动力学的特征是有一个持续45-60分钟的延长滞后阶段,这与FITC-葡聚糖群体在细胞内的转运相对应。在追踪期间,内体pH值在大约20分钟内从细胞外pH值下降到4.6-5.0,然后在接下来的20-40分钟内升高到6.0-6.2。只有在这个阶段,FITC-葡聚糖才以假一级动力学释放回培养基中。液泡H(+)-ATP酶参与内体酸化,因为在液泡H(+)-ATP酶部分缺陷的突变株HGR8和在亲本型菌株AX2中,通过该酶的选择性抑制剂巴弗洛霉素A1,酸化过程明显减少。我们的数据表明,内吞货物从内体被引导至次级溶酶体,次级溶酶体通过回收囊泡与质膜活跃相连。